Are senescence and exhaustion intertwined or unrelated processes that compromise immunity?

被引:361
作者
Akbar, Arne N. [1 ]
Henson, Sian M. [1 ]
机构
[1] UCL, Div Infect & Immun, London WC1E 6BT, England
基金
英国惠康基金; 英国生物技术与生命科学研究理事会;
关键词
CD8(+) T-CELLS; CHRONIC VIRAL-INFECTION; AKT SER(473) PHOSPHORYLATION; B-VIRUS INFECTION; HUMAN CD8+T CELLS; REPLICATIVE SENESCENCE; CELLULAR SENESCENCE; IN-VIVO; DISEASE PROGRESSION; TELOMERE EROSION;
D O I
10.1038/nri2959
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Can the immune system be reactivated continuously throughout the lifetime of an organism or is there a finite point at which repeated antigenic challenge leads to the loss of lymphocyte function or the cells themselves or both? Replicative senescence and exhaustion are processes that control T cell proliferative activity and function; however, there is considerable confusion over the relationship between these two intrinsic cellular control mechanisms. In this Opinion article, we compare the molecular regulation of senescence and exhaustion in T cells. Available data suggest that both processes are regulated independently of each other and that it may be safer to block exhaustion than senescence to enhance immunity.
引用
收藏
页码:289 / 295
页数:7
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